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자료유형
학술저널
저자정보
Park, So-Young (Environmental Toxico-Genomic & Proteomic Center, College of Medicine, Korea University) Woo, Jong-Shick (Department of Immunology, College of Pharmacy, Chung-Ang University) Jung, Yu-Jin (Department of Immunology, College of Pharmacy, Chung-Ang University) Won, Tae-Joon (Department of Immunology, College of Pharmacy, Chung-Ang University) Hih, Yun-Ju (Department of Immunology, College of Pharmacy, Chung-Ang University) Lee, Chan-Woo (Department of Immunology, College of Pharmacy, Chung-Ang University) Kim, Hyo-Shin (Department of Immunology, College of Pharmacy, Chung-Ang University) Joo, Seong-Soo (Research Institute of Veterinary Medicine, Chungbuk University) Lee, Do-Ik (Department of Immunology, College of Pharmacy, Chung-Ang University) Hwang, Kwang-Woo (Department of Immunology, College of Pharmacy, Chung-Ang University)
저널정보
한국응용약물학회 Biomolecules & Therapeutics(구 응용약물학회지) Biomolecules & therapeutics 제16권 제2호
발행연도
2008.1
수록면
126 - 131 (6page)

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Immunosuppressive therapy after organ transplantation is routinely used to prevent rejection of the organ, because this decreases the risk of adverse events, infection, and malignancies. Recently, ursodeoxycholic acid (UDCA), which is isolated from the dried bile of adult Chinese bears, has been shown to reduce the incidence and severity of acute rejection of liver allograft during early phase of liver transplantation. Therefore, in this study, we investigated the effect of UDCA on the proliferation of splenocytes exposed to PMA plus ionomycin. Our results demonstrated that UDCA decreased the splenocytes' proliferation in a dose-dependent manner. The decreased cell proliferation was accompanied with the decreased secretion of cytokines such as IL-2, IFN-${\gamma}$ and TNF-${\alpha}$. In addition, the pretreatment of UDCA on splenocytes stimulated with PMA plus ionomycin decreased the mRNA levels of cytokines (IL-2, IFN-${\gamma}$ and TNF-${\alpha}$) and costimulatory molecules (B7.2 and PD-L1). These results suggest the beneficial effect of UDCA on organ transplantation by decreasing lymphocyte proliferation.

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